Canonical Allele Identifier: CA430114941

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179501492G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178636765G>C , CM000664.2:g.178636765G>C	GRCh38
NC_000002.11:g.179501492G>C , CM000664.1:g.179501492G>C	GRCh37
NC_000002.10:g.179209737G>C	NCBI36
NG_011618.3:g.199038C>G , LRG_391:g.199038C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.33258C>G	ENSP00000343764.6:p.Ala11086=
ENST00000342175.11:c.14343C>G	ENSP00000340554.6:p.Ala4781=
ENST00000359218.10:c.14142C>G	ENSP00000352154.5:p.Ala4714=
ENST00000342175.10:c.14343C>G	ENSP00000340554.6:p.Ala4781=
ENST00000342992.10:c.33258C>G	ENSP00000343764.6:p.Ala11086=
ENST00000359218.9:c.14142C>G	ENSP00000352154.5:p.Ala4714=
ENST00000414766.5:c.2874C>G	ENSP00000401501.1:p.Ala958=
ENST00000460472.6:c.13767C>G	ENSP00000434586.1:p.Ala4589=
ENST00000589042.5:c.40962C>G MANE Select	ENSP00000467141.1:p.Ala13654=
ENST00000591111.5:c.36039C>G	ENSP00000465570.1:p.Ala12013=
ENST00000615779.4:c.36039C>G	ENSP00000483597.1:p.Ala12013=
NM_001256850.1:c.36039C>G	NP_001243779.1:p.Ala12013=
NM_001267550.2:c.40962C>G MANE Select	NP_001254479.2:p.Ala13654=
NM_003319.4:c.13767C>G	NP_003310.4:p.Ala4589=
NM_133378.4:c.33258C>G	NP_596869.4:p.Ala11086=
NM_133432.3:c.14142C>G	NP_597676.3:p.Ala4714=
NM_133437.4:c.14343C>G	NP_597681.4:p.Ala4781=
XM_011511729.1:c.40059C>G	XP_011510031.1:p.Ala13353=
XM_011511730.1:c.13953C>G	XP_011510032.1:p.Ala4651=
XM_011511731.1:c.13812C>G	XP_011510033.1:p.Ala4604=
XM_017004819.1:c.39855C>G	XP_016860308.1:p.Ala13285=
XM_017004820.1:c.35253C>G	XP_016860309.1:p.Ala11751=
XM_017004821.1:c.35250C>G	XP_016860310.1:p.Ala11750=
XM_017004822.1:c.32292C>G	XP_016860311.1:p.Ala10764=
XM_017004823.1:c.13908C>G	XP_016860312.1:p.Ala4636=
XM_024453094.1:c.35403C>G	XP_024308862.1:p.Ala11801=
XM_024453095.1:c.35400C>G	XP_024308863.1:p.Ala11800=
XM_024453096.1:c.34833C>G	XP_024308864.1:p.Ala11611=
XM_024453097.1:c.32175C>G	XP_024308865.1:p.Ala10725=
XM_024453098.1:c.32094C>G	XP_024308866.1:p.Ala10698=
XM_024453099.1:c.13857C>G	XP_024308867.1:p.Ala4619=
XM_024453100.1:c.3711C>G	XP_024308868.1:p.Ala1237=